Patients with isolated or syndromic aniridia carrying chromosomal deletions in 11p13.

Tooth agenesis is one of the most common developmental anomalies in humans and can affect dental occlusion and speech pronunciation. Research has identified an association...

Summary of published mutations in MSX1 gene.

Asterisks indicate the missing teeth. The column shows the sum of missing teeth, in parentheses missing teeth plus third molars are given (I…incisors, C…canines, P…premolars,...

An increasing number of studies have reported unexpectedly high body burdens of triphenyltin (TPT) in wild fishes around the world. To assess the effects of TPT on fish, we...

The Processor for Analyzing XENON (PAX) is used for digital signal processing and event reconstruction of the XENON1T raw data. 

MSX1 homeodomain missense variants in subphenotypes of increasing severity of non-syndromic tooth agenesis (NSTA) and alterations in hydrogen bonds.

Amino-acid sequence for non-mutant and mutant Msx1 homeodomain used for homology modelling.